Evidence map›Paper›PMID 41121943›Full record

SynthesisBrain and behavior2025

Genetic Basis of the Negative Response to the Use of Triptans for the Treatment of Migraine-A Systematic Review and Meta-Analysis.

Victoria Gomes Andreata, Ruan Pablo Duarte Freitas, Jéssica da Silva Nascimento, Patrícia Sodré Araújo, Felipe Eustáquio Dos Santos Guedes, João Vítor Benjamim Pires, Narel Moita Carneiro Nogueira Falcão, Natasha da Silva Leitão, Alcylene Carla de Jesus Dos Santos, Ana Patrícia Pascoal Queiroz and 5 more

Erratum issuedAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Brain and behavior, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Victoria Gomes AndreataHospital Municipal Doutor Waldemar Tebaldi, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-2720-2230
Ruan Pablo Duarte FreitasFaculdade ZARNS, Bahia, Brazil.ORCID https://orcid.org/0000-0001-9881-7016
Jéssica da Silva NascimentoPrograma De Pós-Graduação em Ciências Farmacêuticas (PGFARMA), UNEB, Salvador, Bahia, Brazil.ORCID https://orcid.org/0009-0002-9048-2930
Patrícia Sodré AraújoUniversidade do Estado da Bahia, DCV, UNEB, Salvador, Bahia, Brazil.ORCID https://orcid.org/0000-0001-5843-5662
Felipe Eustáquio Dos Santos GuedesCentro Universitário Dom Pedro II, UNIDOMPEDRO/AFYA, Salvador, Bahia, Brazil.ORCID https://orcid.org/0009-0004-9021-0956
João Vítor Benjamim PiresUniversidade Federal da Bahia (UFBA), Salvador, Bahia, Brazil.ORCID https://orcid.org/0009-0009-5298-7349
Narel Moita Carneiro Nogueira FalcãoHospital Macrorregional de Caxias Dr. Everaldo Aragão, Maranhão, Brazil.ORCID https://orcid.org/0000-0003-2906-5740
Natasha da Silva LeitãoGrupo da Dor Orofacial do Amazonas (DOFAM), Manaus, Amazonas, Brazil.ORCID https://orcid.org/0009-0009-3721-484X
Alcylene Carla de Jesus Dos SantosUniversidade do Estado da Bahia, DCV, UNEB, Salvador, Bahia, Brazil.ORCID https://orcid.org/0000-0002-0074-6000
Ana Patrícia Pascoal QueirozPrograma de Pós-Graduação em Saúde Coletiva (PPGSC), UNEB, Salvador, Bahia, Brazil.ORCID https://orcid.org/0000-0002-1951-6360
Astria Ferrão Dias GonzalesUniversidade do Estado da Bahia, DCV, UNEB, Salvador, Bahia, Brazil.ORCID https://orcid.org/0000-0003-4144-5244
Maica Matos LeãoFaculdade ZARNS, Bahia, Brazil.ORCID https://orcid.org/0009-0004-7262-5242
Emília Katiane Embiruçu de Araújo LeãoUniversidade do Estado da Bahia, DCV, UNEB, Salvador, Bahia, Brazil.ORCID https://orcid.org/0000-0001-5387-6418
Juliana Côrtes FreitasUniversidade do Estado da Bahia, DCV, UNEB, Salvador, Bahia, Brazil.ORCID https://orcid.org/0000-0002-7798-1754
Acássia Benjamim Leal PiresUniversidade do Estado da Bahia, DCV, UNEB, Salvador, Bahia, Brazil.ORCID https://orcid.org/0000-0002-0225-0359

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMigraine is a widespread and disabling neurological disorder, and triptans are a primary treatment for acute episodes. However, around 40% of patients are non-responsive. Genetic polymorphisms can influence drug effectiveness, and several association studies exist. This systematic review consolidates findings from etiological studies, which may provide greater certainty about their use in predicting the risk of low response to triptans.

methodThis study followed COSMOS-E guidelines and employed databases like PubMed, Web of Science, and Embase until 2023. The Newcastle-Ottawa Scale (NOS) was used to assess quality, and statistical meta-analysis was performed.

resultsA comprehensive literature search identified 1421 articles from which 30 met eligibility for full-text review, and 9 studies were included in the final analysis. Although the overall analysis did not confirm a statistically significant association, subgroup analyses demonstrated significant relationships between SLC6A4, 5-HT1B, and COMT polymorphisms and triptan nonresponse, while CALCA and PRDM16 had moderate evidence, and GRIA1 and SCN1A polymorphisms exhibited limited evidence for non-response. While our analysis revealed that genetic polymorphisms are an essential cause of heterogeneity in response to triptans, the included studies showed substantial variability and methodological inconsistency. Polygenic risk scores (PRS) and combined genetic approaches, including prospective clinical trials and multi‑omics integration, can help stratify triptan nonresponders and inform decision‑making in precision and personalized medicine (PPM).

conclusionsThese results underscore the potential utility of these genetic associations in tailored migraine therapy and reinforce the involvement of serotonergic and dopaminergic pathways in triptan efficacy. Future studies with larger and more homogeneous cohorts are essential to validate these associations. Still, clinical implementation of polygenic risk score (PRS) may offer a more effective pathway for applying PPM in migraine care.

Indexed as

Migraine DisordersTryptaminesCatechol O-MethyltransferaseHumansPolymorphism, GeneticSerotonin Plasma Membrane Transport ProteinsCatechol O-MethyltransferaseSerotonin Plasma Membrane Transport ProteinsSLC6A4 protein, humanTryptaminesgenetic polymorphismsmigraine disorderspharmacogeneticstryptamines

Identifiers

PMID41121943
PMCPMC12541135

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.